Quasar Electronics Technology (Dongguan) Co., Ltd.
Registered establishment in Dongguan, Guangdong, China. 2 device types.
Quasar Electronics Technology (Dongguan) Co., Ltd. is a contract manufacturer holding a current FDA establishment registration. The registration covers Cuff, Tracheal Tube, Inflatable, Catheter, Peripheral, Atherectomy. Its earliest product listing with the FDA dates from 2015.
Registration
| Status | Registered |
|---|---|
| Registration expires | 2026 |
| Registration number | 3014254831 |
| FEI number | 3014254831 |
| Establishment type | Contract manufacturer, Manufacturer |
Location
| City | Dongguan |
|---|---|
| Province | Guangdong |
| Address | Bldg 8 of Guantai Biotech Technical Cooperation center Taoyuan 1st Rd |
| Postal code | 523808 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Catheter, Peripheral, Atherectomy | Class 2 | Auryon Atherectomy System OR Auryon Atherecomy Catheter | 2022 | 3 |
| Cuff, Tracheal Tube, Inflatable | Class 2 | Cuff Pressure Manometer | 2015 | 6 |
From the Company
Published by the company on its own website, not by the FDA.
| Founded | 1988 |
|---|---|
| Employees | 3000 |
| Factory area | 4400 m2 |
| Main products | Medical device assembly, Molding, Packaging, Quality testing |
| Certifications | ISO 13485 |
| Export markets | Global |
| OEM and ODM | Offered |
Nearby Manufacturers
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.
The manufacturer named here can complete this record.